ClinVar Miner

List of variants reported as uncertain significance for atrial fibrillation (disease) by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_000218.2(KCNQ1):c.296C>G (p.Pro99Arg) rs370435862
NM_000335.4(SCN5A):c.1282G>A (p.Glu428Lys) rs199473111
NM_000335.4(SCN5A):c.152C>T (p.Ala51Val) rs727505131
NM_000335.4(SCN5A):c.2399G>A (p.Arg800His) rs566251672
NM_000335.4(SCN5A):c.2924G>A (p.Arg975Gln) rs753149586
NM_000335.4(SCN5A):c.3080G>A (p.Arg1027Gln) rs763891399
NM_000335.4(SCN5A):c.3118G>A (p.Gly1040Arg) rs199473186
NM_000335.4(SCN5A):c.3553G>A (p.Ala1185Thr) rs199473595
NM_000335.4(SCN5A):c.4783T>A (p.Phe1595Ile) rs199473278
NM_000335.4(SCN5A):c.5686C>T (p.Arg1896Trp) rs45465995
NM_000335.4(SCN5A):c.5735G>A (p.Arg1912His) rs199473327
NM_000335.4(SCN5A):c.5783G>A (p.Arg1928His) rs727504822
NM_000335.4(SCN5A):c.5792C>T (p.Ala1931Val)
NM_000335.4(SCN5A):c.5800G>A (p.Gly1934Ser) rs199473637
NM_000335.4(SCN5A):c.5901C>G (p.Ile1967Met) rs199473333
NM_000335.4(SCN5A):c.880G>A (p.Val294Met) rs199473086
NM_001037.5(SCN1B):c.134G>A (p.Arg45His) rs180943300
NM_001037.5(SCN1B):c.158C>A (p.Thr53Asn) rs1568348711
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro) rs786205834
NM_002234.4(KCNA5):c.797C>T (p.Thr266Ile)
NM_002234.4(KCNA5):c.79G>A (p.Gly27Ser) rs201238766
NM_005691.3(ABCC9):c.1012-7G>A rs727502874
NM_005691.3(ABCC9):c.2312C>T (p.Thr771Ile) rs180739851
NM_006172.4(NPPA):c.253G>A (p.Gly85Arg) rs749353276
NM_181703.4(GJA5):c.995G>A (p.Arg332His) rs116551187
NM_181798.1(KCNQ1):c.1174C>T (p.Arg392Cys) rs199472787
NM_181798.1(KCNQ1):c.133G>A (p.Val45Met) rs199472694
NM_181798.1(KCNQ1):c.1480G>A (p.Gly494Ser) rs199472820
NM_181798.1(KCNQ1):c.1504G>A (p.Gly502Ser) rs775608046
NM_181798.1(KCNQ1):c.263T>G (p.Val88Gly) rs368011737
NM_181798.1(KCNQ1):c.747+5G>A rs76735093
NM_181798.1(KCNQ1):c.973C>T (p.Arg325Trp) rs140452381
NM_181798.1(KCNQ1):c.974G>A (p.Arg325Gln) rs145229963

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